Canonical Allele Identifier: PA2827936695
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly223Ser
CA367401165
NM_001354800.1:c.667G>A